rs49430385 SNP Detail

Summary

• ID
  rs49430385
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:103911050 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AGGAAATTTG TTTTAATTTG AGAAAGGAAA TGAGTCAGGG
  AGTGGGGGGG AAATCTAGAG GGAGAAGGGA AGTATGGAAG AAATGCAGCT GAGGTGCAGT
  T
  ACTAGGTGGG TGGGAAGTGT GCTCCTTGCC CTCTGAGCTC TTGAAAACTG CCATTCTCCT
  GGAATCCACA TAACCTAGAA AGAATTCAGC AGGAGGGGG                       
  
  T = T
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

  ---

SNP Assays
and
SNP Consensus

Strain alleles of submitted assays, and consensus values for this SNP

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	DBA/2J
ss147142879	ENSMUSSNP2067641	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs49430385					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:103911050 () rs orientation: forward

Symbol	Name	Function Class
Cd59b	CD59b antigen	Intron
Rr562020	regulatory region 562020	1581 bp distal
Rr562021	regulatory region 562021	824 bp proximal
Rr562022	regulatory region 562022	1846 bp proximal